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Olympus Corporation of the Americas recalls TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP, Model Number: LF-GP
Recalled December 20, 2023 · FDA recall Z-0557-2024 · Olympus Corporation of the Americas
Hazard
Fiberscopes do not have adequate data to support that the suction flow rate meets the device specification. · FDA Class II
Units
75
Sold at
Worldwide - US Nationwide distribution in the states of AK, AL, AZ, CA, GA, IL, IN, MA, MD, MI, NC, NJ, OH, TX, UT, VA, WA, WV & AP (Armed Forces Pacific) and the countries of OUS: EMEA, Japan and Australia.
Description
Fiberscopes do not have adequate data to support that the suction flow rate meets the device specification.
Product
TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP, Model Number: LF-GP
Manufacturer(s)
Olympus Corporation of the Americas
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →